Cardiogenic Shock Working Group Registry

Description

The Cardiogenic Shock Working Group is a multicenter registry where we collect de-identified clinical variables from the medical records and follow-up phone calls of shock patients from multiple institutions and centralize this data to a single registry for analysis of clinical outcomes.

Conditions

Cardiogenic Shock

Study Overview

Study Details

Study overview

The Cardiogenic Shock Working Group is a multicenter registry where we collect de-identified clinical variables from the medical records and follow-up phone calls of shock patients from multiple institutions and centralize this data to a single registry for analysis of clinical outcomes.

Cardiogenic Shock Working Group Registry

Cardiogenic Shock Working Group Registry

Condition
Cardiogenic Shock
Intervention / Treatment

-

Contacts and Locations

Weston

Cleveland Clinic Florida, Weston, Florida, United States, 33331

Chicago

Northwestern Medicine, Chicago, Illinois, United States, 60611

Chicago

University of Chicago, Chicago, Illinois, United States, 60612

Portland

Maine Medical Center, Portland, Maine, United States, 04102

Boston

Tufts Medical Center, Boston, Massachusetts, United States, 02111

Boston

Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States, 02215

Hackensack

Hackensack Meridian Health, Hackensack, New Jersey, United States, 07601

New York

Columbia University Irving Medical Center, New York, New York, United States, 10032

Portland

Providence St. Vincent Heart Clinic, Portland, Oregon, United States, 97225

Pittsburgh

Allegheny General Hospital, Pittsburgh, Pennsylvania, United States, 15212

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Patients must have cardiogenic shock.
  • 1. At least 2 of the following concurrently at any point during the index hospitalization:
  • * Cardiac Index \< 2.2
  • * PAPI \< 1.0
  • * Cardiac Power Output ≤ 0.6
  • * MAP \< 60mmHg or a \>30mmHg drop in MAP from baseline
  • * SBP \< 90mmHg or a \>30mmHg drop in SBP from baseline
  • * Pulse \> 100
  • 2. Require at least one acute mechanical circulatory support device, vasopressor or inotrope to maintain values above the above target.

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Tufts Medical Center,

Reshad Garan, MD, STUDY_DIRECTOR, Beth Israel Deaconess Medical Center

Claudius Mahr, DO, STUDY_DIRECTOR, University of Washington

Jaime Hernandez-Montfort, MD, STUDY_DIRECTOR, Cleveland Clinic Foundation-Florida

Daniel Burkhoff, MD PhD, STUDY_DIRECTOR, CardioVascular Research Foundation

Study Record Dates

2025-06-01